Canonical Allele Identifier: CA15839702

Gene: CYP1A1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74723851G>A , CM000677.2:g.74723851G>A	GRCh38
NC_000015.9:g.75016192G>A , CM000677.1:g.75016192G>A	GRCh37
NC_000015.8:g.72803245G>A	NCBI36
NG_008431.1:g.6310G>A
NG_008431.2:g.6310G>A
NG_061374.1:g.6678C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.-29-725C>T MANE Select	ENSP00000369050.3:n.-29-725C>T
ENST00000379727.7:c.-29-725C>T	ENSP00000369050.3:n.-29-725C>T
ENST00000395048.6:c.-26-728C>T	ENSP00000378488.2:n.-26-728C>T
ENST00000395049.8:c.-29-725C>T	ENSP00000378489.4:n.-29-725C>T
ENST00000562201.5:c.-26-728C>T	ENSP00000455340.1:n.-26-728C>T
ENST00000564596.5:c.-220-1317C>T	ENSP00000457668.1:n.-220-1317C>T
ENST00000566503.1:c.-220-1317C>T	ENSP00000455846.1:n.-220-1317C>T
ENST00000567032.5:c.-29-725C>T	ENSP00000456585.1:n.-29-725C>T
ENST00000569630.5:c.-26-728C>T	ENSP00000455051.1:n.-26-728C>T
ENST00000617691.4:c.-26-728C>T	ENSP00000482863.1:n.-26-728C>T
NM_000499.3:c.-26-728C>T	NP_000490.1:n.-26-728C>T
XM_005254185.1:c.-29-725C>T	XP_005254242.1:n.-29-725C>T
NM_000499.5:c.-26-728C>T	NP_000490.1:n.-26-728C>T
NM_001319216.2:c.-29-725C>T	NP_001306145.1:n.-29-725C>T
NM_001319217.2:c.-29-725C>T MANE Select	NP_001306146.1:n.-29-725C>T